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&Figures 2016
WA
37,770 NH
MT 8,680 ME
ND VT
6,070 9,270
3,930 MN 4,050
OR
29,130
22,510 MA
ID
SD WI NY 37,620
8,120
4,690 32,970 110,280
WY RI
MI
2,920 6,190
56,530
IA PA
NV NE 17,100 83,560 CT 21,700
14,390 9,740 OH NJ 49,750
UT IL IN 66,020
CA 11,030 65,090 35,180 DE 5,630
CO WV
173,200 24,730 KS 11,770 VA MD 30,990
MO 43,190
14,530 KY
34,270 DC 2,910
25,720
NC
TN 54,450
AZ OK 37,650
32,510 NM 19,650 AR SC
9,750 16,460 27,980
MS AL GA
16,680 27,020 48,670
TX
116,690 LA
25,070
AK
3,330 FL
121,240
US
1,685,210
PR
HI N/A
6,850
Estimated numbers of new cancer cases for 2016, excluding basal cell and squamous cell skin cancers and in situ carcinomas except urinary bladder.
Estimates are not available for Puerto Rico.
Note: State estimates are offered as a rough guide and should be interpreted with caution. State estimates may not add to US total due to rounding.
Selected Cancers 9
Figure 3. Leading Sites of New Cancer Cases and Deaths 2016 Estimates 10
Table 6. Probability (%) of Developing Invasive Cancer during Selected Age Intervals by Sex, US, 2010-2012 14
Table 7. Trends in 5-year Relative Survival Rates (%) by Race, US, 1975-2011 18
Table 8. Five-year Relative Survival Rates (%) by Stage at Diagnosis, US, 2005-2011 21
Tobacco Use 43
Figure 4. Number and Percentage (%) of Cancer Deaths Attributable to Cigarette Smoking in 2011,
Adults 35 Years and Older 43
Cancer Disparities 50
Table 9. Incidence and Death Rates for Selected Cancers by Site, Race, and Ethnicity, US, 2008-2012 51
Figure 5. Geographic Patterns in Lung Cancer Death Rates by State, US, 2008-2012 52
Sources of Statistics 64
American Cancer Society Recommendations for the Early Detection of Cancer in Average-risk
Asymptomatic People 66
Suggested citation: American Cancer Society. Cancer Facts & Figures 2016. Atlanta: American Cancer Society; 2016.
How Many People Alive Today Have
Basic Cancer Facts Ever Had Cancer?
Nearly 14.5 million Americans with a history of cancer were alive
on January 1, 2014. Some of these individuals were diagnosed
What Is Cancer? recently and undergoing treatment, while most were diagnosed
Cancer is a group of diseases characterized by the uncontrolled many years ago with no current evidence of cancer.
growth and spread of abnormal cells. If the spread is not con-
trolled, it can result in death. Cancer is caused by external
factors, such as tobacco, infectious organisms, and an unhealthy
How Many New Cases and Deaths
diet, and internal factors, such as inherited genetic mutations, Are Expected to Occur This Year?
hormones, and immune conditions. These factors may act About 1,685,210 new cancer cases are expected to be diagnosed
together or in sequence to cause cancer. Ten or more years often in 2016 (Table 1, page 4). This estimate does not include car-
pass between exposure to external factors and detectable can- cinoma in situ (noninvasive cancer) of any site except urinary
cer. Treatments include surgery, radiation, chemotherapy, bladder, nor does it include basal cell or squamous cell skin can-
hormone therapy, immune therapy, and targeted therapy (drugs cers because these are not required to be reported to cancer
that interfere specifically with cancer cell growth). registries. Table 2 (page 5) provides estimated new cancer
cases in 2016 by state.
Can Cancer Be Prevented? About 595,690 Americans are expected to die of cancer in 2016,
A substantial proportion of cancers could be prevented. All can- which translates to about 1,630 people per day (Table 1, page
cers caused by tobacco use and heavy alcohol consumption 4). Cancer is the second most common cause of death in the
could be prevented completely. In 2016, about 188,800 of the esti- US, exceeded only by heart disease, and accounts for nearly 1 of
mated 595,690 cancer deaths in the US will be caused by cigarette every 4 deaths. Table 3 (page 6) provides estimated cancer
smoking, according to a recent study by American Cancer Soci- deaths by state in 2016.
ety epidemiologists. In addition, the World Cancer Research
Fund estimates that about 20% of all cancers diagnosed in the How Much Progress Has Been Made
US are related to body fatness, physical inactivity, excess alcohol
consumption, and/or poor nutrition, and thus could also be pre-
in the Fight against Cancer?
vented. Certain cancers are related to infectious agents, such as Trends in cancer death rates are the best measure of progress
human papillomavirus (HPV), hepatitis B virus (HBV), hepatitis against cancer. The total cancer death rate rose for most of the
C virus (HCV), human immunodeficiency virus (HIV), and Heli- 20th century because of the tobacco epidemic, peaking in 1991
cobacter pylori (H. pylori). Many of these cancers could be avoided at 215 cancer deaths per 100,000 persons. However, from 1991 to
by preventing these infections through behavioral changes or 2012, the rate dropped 23% because of reductions in smoking, as
vaccination, or by treating the infection. Many of the more than well as improvements in early detection and treatment. This
5 million skin cancer cases that are diagnosed annually could be decline translates into the avoidance of more than 1.7 million
prevented by protecting skin from excessive sun exposure and cancer deaths. Death rates are declining for all four of the most
not using indoor tanning devices. common cancer types lung, colorectal, breast, and prostate
(Figure 1, page 2 and Figure 2, page 3).
Screening can prevent colorectal and cervical cancers by allow-
ing for the detection and removal of precancerous lesions.
Screening also offers the opportunity to detect some cancers Do Cancer Incidence and Death Rates
early, when treatment is less extensive and more likely to be suc- Vary By State?
cessful. Screening is known to help reduce mortality for cancers Tables 4 (page 7) and 5 (page 8) provide average annual
of the breast, colon, rectum, cervix, and lung (among long-term incidence and death rates during 2008 to 2012 for selected cancer
and/or heavy smokers). In addition, a heightened awareness of types by state. For some cancers (e.g., lung), there is substantial
changes in certain parts of the body, such as the breast, skin, variation by state, whereas for others (e.g., breast), there is less
mouth, eyes, or genitalia, may also result in the early detection of variation. For more information about geographic disparities in
cancer. For complete cancer screening guidelines, see page 66. cancer occurrence, see page 53.
Figure 1. Trends in Age-adjusted Cancer Death Rates* by Site, Males, US, 1930-2012
100
80
Rate per 100,000 male population
60
Stomach Prostate
Colon & rectum
40
20
Liver Pancreas
Leukemia
0
1930 1935 1940 1945 1950 1955 1960 1965 1970 1975 1980 1985 1990 1995 2000 2005 2012
*Per 100,000, age adjusted to the 2000 US standard population. Mortality rates for pancreatic and liver cancers are increasing.
Note: Due to changes in ICD coding, numerator information has changed over time. Rates for cancers of the liver, lung and bronchus, and colon and rectum are affected
by these coding changes.
Source: US Mortality Volumes 1930 to 1959 and US Mortality Data 1960 to 2012, National Center for Health Statistics, Centers for Disease Control and Prevention.
2016, American Cancer Society, Inc., Surveillance Research
Figure 2. Trends in Age-adjusted Cancer Death Rates* by Site, Females, US, 1930-2012
100
80
Rate per 100,000 female population
60
40
Breast
Colon & rectum
Stomach Uterus
20
Pancreas
Liver
0
1930 1935 1940 1945 1950 1955 1960 1965 1970 1975 1980 1985 1990 1995 2000 2005 2012
*Per 100,000, age adjusted to the 2000 US standard population. Uterus refers to uterine cervix and uterine corpus combined. Mortality rates for pancreatic and liver
cancers are increasing.
Note: Due to changes in ICD coding, numerator information has changed over time. Rates for cancers of the liver, lung and bronchus, and colon and rectum are affected
by these coding changes.
Source: US Mortality Volumes 1930 to 1959, US Mortality Data 1960 to 2012, National Center for Health Statistics, Centers for Disease Control and Prevention.
2016, American Cancer Society, Inc., Surveillance Research
Selected Cancers
This section provides basic information on risk factors, symp- Less common symptoms include other persistent changes to the
toms, early detection, and treatment, as well as statistics on breast, such as thickening, swelling, distortion, tenderness, skin
incidence, mortality, and survival, for the most commonly diag- irritation, redness, scaliness, nipple abnormalities, or spontane-
nosed cancers. The information primarily applies to the more ous discharge. Breast pain is more likely to be caused by benign
common subtypes for each site and may have limited relevance conditions and is not a common symptom of breast cancer.
to rare subtypes.
Risk factors: Potentially modifiable factors associated with
increased breast cancer risk include weight gain after the age of
Breast 18 and/or being overweight or obese (for postmenopausal breast
New cases: In 2016, invasive breast cancer will be diagnosed in cancer), use of menopausal hormone therapy (combined estro-
about 246,660 women and 2,600 men. An additional 61,000 new gen and progestin), physical inactivity, and alcohol consumption.
cases of in situ breast cancer will be diagnosed in women. Breast In addition, recent research indicates that long-term, heavy
cancer is the most frequently diagnosed cancer in women (Fig- smoking may also increase breast cancer risk, particularly
ure 3, page 10). among women who start smoking before their first pregnancy.
The International Agency for Research on Cancer has concluded
Incidence trends: From 2003 to 2012, the most recent 10 years that shift work, particularly at night (i.e., that disrupts sleep pat-
for which data are available, breast cancer incidence rates were terns), may be associated with an increased risk of breast cancer.
stable in white women and increased slightly (by 0.3% per year)
in black women, resulting in the convergence of rates in blacks Non-modifiable factors associated with increased breast cancer
with those in whites. risk include older age; a personal or family history of breast or
ovarian cancer; inherited mutations (genetic alterations) in
Deaths: An estimated 40,890 breast cancer deaths (40,450 women, BRCA1, BRCA2, or other breast cancer susceptibility genes; cer-
440 men) are expected in 2016. Breast cancer ranks second as a tain benign breast conditions (such as atypical hyperplasia); a
cause of cancer death in women. history of ductal or lobular carcinoma in situ; high-dose radia-
Mortality trends: From 2003 to 2012, breast cancer death rates tion to the chest at a young age (e.g., for cancer treatment); high
decreased by 1.9% per year in white women and by 1.4% per year breast tissue density (the amount of glandular tissue relative to
in black women. Overall, breast cancer death rates declined by fatty tissue measured on a mammogram); high bone mineral
36% from 1989 to 2012 due to improvements in early detection density (evaluated during screening for osteoporosis); and type
and treatment, translating to the avoidance of approximately 2 diabetes (independent of obesity). Reproductive factors that
249,000 breast cancer deaths. increase risk include a long menstrual history (menstrual peri-
ods that start early and/or end later in life), recent use of oral
Signs and symptoms: The most common symptom of breast contraceptives, never having children, having ones first child
cancer is a lump or mass in the breast, which is often painless. after age 30, and high natural levels of sex hormones.
Estimates are rounded to the nearest 10, and cases exclude basal cell and squamous cell skin cancers and in situ carcinoma except urinary bladder.
2016, American Cancer Society, Inc., Surveillance Research
Factors associated with a decreased risk include breastfeeding at age 30. For more information on breast cancer screening, see
for at least one year, regular moderate or vigorous physical activ- the American Cancer Societys screening guidelines on page 66.
ity, and maintaining a healthy body weight. Two medications
Treatment: Taking into account tumor characteristics, includ-
tamoxifen and raloxifene have been approved to reduce breast
ing size and extent of spread, as well as patient preference,
cancer risk in women at high risk. Raloxifene appears to have a
treatment usually involves either breast-conserving surgery
lower risk of certain side effects, but is only approved for use in
(surgical removal of the tumor and surrounding tissue) or mas-
postmenopausal women.
tectomy (surgical removal of the breast). For early breast cancer
Early detection: Mammography is a low-dose x-ray procedure (without spread to the skin, chest wall, or distant organs),
used to detect breast cancer at an early stage. Numerous studies long-term survival is similar for women treated with breast-
have shown that early detection with mammography helps save conserving surgery plus radiation therapy and those treated
lives and increases treatment options. However, like any screen- with mastectomy. Underarm lymph nodes are usually removed
ing tool, mammography is not perfect. For example, it can miss and evaluated during surgery to determine whether the tumor
cancers, particularly those in women with very dense breasts, has spread beyond the breast. Women undergoing mastectomy
and also detects cancers that would never have caused harm, who elect breast reconstruction have several options, including
resulting in some overdiagnoses. Most (95%) of the 10% of women the tissue or materials used to restore breast shape and the tim-
who have an abnormal mammogram do not have cancer. For ing of the procedure.
women at average risk of breast cancer, recently updated Ameri-
Treatment may also involve radiation therapy, chemotherapy
can Cancer Society screening guidelines recommend that those
(before or after surgery), hormonal therapy, and/or targeted
40 to 44 years of age have the choice for annual mammography;
therapy. Women with early stage breast cancer that tests posi-
those 45 to 54 have annual mammography; and those 55 years of
tive for hormone receptors benefit from treatment with
age and older have biennial or annual mammography, continu-
hormonal therapy for at least 5 years. For women whose cancer
ing as long as their overall health is good and life expectancy is
overexpresses the growth-promoting protein HER2, several tar-
10 or more years. For some women at high risk of breast cancer,
geted therapies are available.
annual screening using magnetic resonance imaging (MRI) in
addition to mammography is recommended, typically starting
Some risk factors are most closely associated with specific types Some of these drugs are also used to treat a type of ALL involv-
of leukemia. For example, family history is a strong risk factor ing a similar genetic defect. People diagnosed with CLL that is
for CLL. Cigarette smoking is a risk factor for AML in adults, and not progressing or causing symptoms may not require treat-
there is accumulating evidence that parental smoking before ment. For those who do require treatment, CLL-targeted drugs
and after childbirth may increase the risk of childhood leuke- are effective for some patients, even when other treatments are
mia. There is limited evidence that maternal exposure to paint no longer working. Certain types of leukemia may be treated
fumes also increases the risk of childhood leukemia. Exposure with high-dose chemotherapy followed by stem cell transplanta-
to certain chemicals, such as formaldehyde and benzene, tion under appropriate conditions.
increases the risk of myeloid leukemia. Infection with human
Survival: Survival rates vary substantially by leukemia subtype,
T-cell leukemia virus type I (HTLV-I) can cause a rare type of
ranging from a current (2005-2011) 5-year relative survival of
leukemia called adult T-cell leukemia/lymphoma. The preva-
26% for patients diagnosed with AML to 82% for those with CLL.
lence of HTLV-I infection is most common in southern Japan and
Advances in treatment have resulted in a dramatic improve-
the Caribbean, and infected individuals in the US tend to be
ment in survival over the past three decades for most types of
immigrants (or their descendants) from these regions.
leukemia (Table 7, page 18). For example, from 1975-1977 to
Early detection: There are no recommended screening tests for 2005-2011, the overall 5-year relative survival for ALL increased
the early detection of leukemia. However, it is sometimes diag- from 41% to 70%. In large part due to the discovery of targeted
nosed early because of abnormal results on blood tests performed drugs, the 5-year survival rate for CML has doubled over the past
for other indications. two decades, from 31% in the early 1990s to 63% for patients
diagnosed from 2005 to 2011. Survival rates beyond 5 years are
Treatment: Chemotherapy is used to treat most types of leuke-
more relevant for chronic than for acute leukemia because of the
mia. Various anticancer drugs are used, either in combination or
slow-growing nature of chronic disease. For example, the abso-
as single agents. Several targeted drugs are effective for treating
lute drop in the survival rate from 5 to 10 years following
CML because they attack cells with the Philadelphia chromo-
diagnosis is 15 percentage points for chronic leukemia versus 3
some, the genetic abnormality that is the hallmark of CML.
points for acute leukemia.
use of menopausal hormone therapy (estrogen alone and estro- ing ovarian cancer mortality when used as a screening tool in
gen combined with progesterone) also increases risk. Tobacco average-risk women.
smoking increases the risk of a rare type of ovarian cancer
Treatment: Treatment includes surgery and often chemother-
(mucinous). Pregnancy, long-term use of oral contraceptives,
apy. Surgery usually involves removal of both ovaries and
and tubal ligation reduce risk.
fallopian tubes (salpingo-oophorectomy), the uterus (hysterec-
Early detection: There is currently no sufficiently accurate tomy), and the omentum (fatty tissue attached to some of the
screening test for the early detection of ovarian cancer in aver- organs in the belly), along with biopsies of the peritoneum (lin-
age-risk women. A pelvic exam, sometimes in combination with ing of the abdominal cavity). In younger women with very early
a transvaginal ultrasound, may be used to evaluate women with stage tumors who want to preserve fertility, only the involved
symptoms, but only occasionally detects ovarian cancer, gener- ovary and fallopian tube may be removed. Among patients with
ally when the disease is advanced. For women who are at high early ovarian cancer, more accurate surgical staging (micro-
risk, a thorough pelvic exam in combination with transvaginal scopic examination of tissue from different parts of the pelvis and
ultrasound and a blood test for the tumor marker CA125 may be abdomen) has been associated with better outcomes. For some
offered, although this strategy has not proven effective in reduc- women with advanced disease, chemotherapy administered
Mortality trends: Although overall mortality rates have been Prevention: Minimize skin exposure to intense UV radiation by
stable since the late 1980s, these trends also vary by age. While seeking shade; wearing protective clothing (long sleeves, long
rates in individuals younger than 50 have been declining by 2.6% pants or skirts, tightly woven fabric, and a wide-brimmed hat);
per year since 1986, they have been increasing by 0.6% per year wearing sunglasses that block ultraviolet rays; applying broad-
since 1990 among those 50 and older. spectrum sunscreen that has a sun protection factor (SPF) of 30
or higher to unprotected skin; and not sunbathing or indoor tan-
Signs and symptoms: Warning signs of skin cancer include
ning. Children should be especially protected from the sun
changes in the size, shape, or color of a mole or other skin lesion,
because severe sunburns in childhood may greatly increase the
the appearance of a new growth on the skin, or a sore that doesnt
risk of melanoma. In July 2014, the US Surgeon General released
heal. Changes that progress over a month or more should be
a Call to Action to Prevent Skin Cancer, citing the elevated and
evaluated by a health care provider. Basal cell carcinoma may
growing burden of this disease. The purpose of this initiative is
appear as a growth that is flat, or as a small, raised pink or red
to increase awareness and encourage all Americans to engage in
translucent, shiny area that may bleed following minor injury.
behaviors that reduce the risk of skin cancer. See surgeongeneral.
Squamous cell carcinoma may appear as a growing lump, often
gov/library/calls/prevent-skin-cancer/call-to-action-prevent-skin-
with a rough surface, or as a flat, reddish patch that grows
cancer.pdf for more information.
slowly.
Early detection: The best way to detect skin cancer early is to
Risk factors: For melanoma, major risk factors include a per-
recognize new or changing skin growths, particularly those that
sonal or family history of melanoma and the presence of atypical,
look different from other moles. All major areas of the skin
large, or numerous (more than 50) moles. High exposure to
should be examined regularly, and any new or unusual lesions,
ultraviolet (UV) radiation, from sunlight or use of indoor tan-
or a progressive change in a lesions appearance (size, shape, or
ning, is a major risk factor for all types of skin cancer. (The
color, etc.), should be evaluated promptly by a physician. The
International Agency for Research on Cancer has classified
ABCDE rule outlines warning signs of the most common type of
indoor tanning devices as carcinogenic to humans based on an
melanoma: A is for asymmetry (one half of the mole does not
extensive review of scientific evidence.) People at highest risk
match the other half); B is for border irregularity (the edges are
include those with sun sensitivity (e.g., sunburning easily, diffi-
ragged, notched, or blurred); C is for color (the pigmentation is
culty tanning, or natural blond or red hair color); a history of
not uniform, with variable degrees of tan, brown, or black); D is
excessive sun exposure, including sunburns; diseases or treat-
for diameter greater than 6 millimeters (about the size of a pen-
ments that suppress the immune system; and a past history of
cil eraser); and E is for evolution. Not all melanomas have these
skin cancer.
signs, so be alert for any new or changing skin growths or spots.
Median age 34 35 34 32 35 34 37 29 29 22 29 27 23
Native 41 39 49 32 37 39 75 37 47 61 51 98 91
Average household size (n of persons) 3.1 2.9 3.4 3.1 3.5 2.7 2.4 4.0 3.9 5.1 3.8 3.2 4.1
Non-English at home 69 74 55 76 83 68 32 84 75 88 75 11 43
Poverty (%) 10 11 6 6 14 12 5 16 20 25 15 13 17
Per capita income ($) 29,630 31,382 26,514 40,221 22,234 27,088 32,923 25,135 16,472 11,938 17,183 20,740 15,021
Cancer is the leading cause of death among AANHPIs, accounting Overall cancer incidence rates declined from 2003 to 2012 (the
for 27% of all deaths (Table S2, page 28). Among non-Hispanic most recent 10 years for which data are currently available)
whites, heart disease remains the leading cause of death, followed among AANHPI males by 1.9% annually, compared with declines
by cancer. However, the cancer death rate in AANHPIs (104.2 per of 1.5% annually among NHW males.9 During the same period,
100,000) is about 40% lower than that in NHWs (170.2). incidence rates remained stable among both AANHPI and NHW
females (Figure S5, page 32). However, mortality rates during
The lifetime probability of developing cancer among AANHPIs is
this period declined among both AANHPI males and females by
36% in males and 33% in females (Table S3, page 29), compared
1.5% and 0.8% annually, respectively, similar to the declines in
to 42% and 38% in NHW males and females, respectively. In 2016,
NHWs.10 Trends in cancer occurrence among Asian Americans
an estimated 57,740 new cancer cases and 16,910 cancer deaths
are influenced not only by the risk factor profiles of those living
will occur among AANHPIs. According to these estimates, the
in the US, but also by the influx of immigrants.
most commonly diagnosed cancers among males are prostate
(18%), lung (14%), and colorectum (12%) (Figure S2, page 29). Overall five-year cancer survival among AANHPIs compared
Among females, the most common cancers are breast (34%), thy- with NHWs is lower for males (62% versus 68%) and similar for
roid (10%), and lung (9%). The three leading causes of cancer females (70% versus 68%; Figure S6, page 33). Survival is notably
death are lung (27%), liver (14%), and colorectum (11%) among higher among AANHPIs for stomach, liver, and nasopharyngeal
males, and lung (21%), breast (14%), and colorectum (11%) among cancers, while it is similar for other major cancer sites (Figure
females. S6, page 33). Survival statistics for minority groups in the US
are particularly influenced by incomplete follow-up of cancer
As mentioned previously, there is substantial variation in cancer
patients due to lost contact or inability to link to death registries,
occurrence among AANHPI subgroups. For both males and
artificially inflating rates by as much as 6 percentage points
females, Samoans and Native Hawaiians have the highest over-
among Asian Americans.11 Lost contact of cancer patients is
all cancer incidence rates, while Asian Indians and Pakistanis
sometimes the result of terminally ill people returning to their
(grouped together) and Cambodians have the lowest rates (Fig-
country of origin. As a result, comparisons of survival between
ure S4, page 31).
racial/ethnic groups should be interpreted with caution.
Major cancer sites increased by 1.1% annually.9 Reasons for this increase are thought
to include changes in factors such as body weight and repro
Female breast ductive patterns following immigration and acculturation.12, 16
Breast cancer is the most commonly diagnosed cancer and the Recent uptake of mammography screening among Asian Amer-
second leading cause of cancer death among AANHPI women, icans may also have contributed.12, 17, 18 Increases in incidence of
with a total of 11,090 new invasive cases and 1,180 deaths in situ breast cancers among AANHPIs since 1992 are consis-
expected to occur in 2016 (Figure S2, page 29). About one in 10 tent with increased screening.19 Breast cancer mortality rates
AANHPI women will be diagnosed with breast cancer in her life- decreased by 1.4% annually from 2003 to 2012 among AANHPI
time (Table S3, page 29). Age-standardized breast cancer women and by 1.9% annually among NHWs.10 These reductions
incidence and mortality rates are 30% and 50% lower, respec- have been attributed to improvements in both treatment and
tively, than those in NHWs (Figure S3, page 30). There is early detection.20
substantial variation in breast cancer occurrence within the
The stage at breast cancer diagnosis is similar in AANHPIs and
AANHPI population, with lower rates among groups that have
NHWs (Figure S8, page 34), although the overall 5-year cause-
immigrated more recently. Incidence rates range from 35.0 (per
specific survival is slightly higher among AANHPI women
100,000) in Cambodian women to 135.9 in Native Hawaiian
(Figure S6, page 33). However, there are some notable differ-
women (Figure S4, page 31). These differences are thought to
ences in survival by nativity and between AANHPI subgroups. A
be related to extent of adoption of western behaviors that
study in California showed that compared with foreign-born
increase breast cancer risk, such as a later age at childbirth,
women, those who are US-born are more likely to be diagnosed
fewer births, and higher body weight.12 A California study found
with breast cancer at a localized stage and have higher survival
breast cancer rates to be generally higher among US-born com-
after adjusting for stage and other prognostic factors.21 Com-
pared to foreign-born Asian American women.13 Breast cancer
pared to NHWs, survival rates are higher in Japanese but lower
incidence rates in AANHPI countries of origin are generally sub-
in NHPIs.22 Factors thought to contribute to the Japanese sur-
stantially lower than in the US;14 however, in many Asian
vival advantage include lower body weight and healthy diet.22, 23
countries, risk among recent generations is approaching that in
Differences in survival between Asian American subgroups may
the US.15
also reflect biological differences in tumor characteristics;24 a
Breast cancer incidence rates among AANHPI women have been study in California showed differing prevalence of breast cancer
increasing gradually since 2005 (Figure S7, page 33). From 2003 subtypes, each with distinct treatment needs and prognosis,
to 2012, in contrast to stable rates in NHWs, rates in AANHPIs among Asian American subgroups.25
Chronic lower respiratory diseases 7 1,624 2.9 12.8 3 127,116 6.3 46.2
Nephritis, nephrotic syndrome & nephrosis 10 1,054 1.9 8.0 10 33,105 1.6 11.8
AANHPI = Asian American, Native Hawaiian, and Pacific Islander. NHW = Non-Hispanic white. Rates are per 100,000 and age-adjusted to the 2000 US standard population.
Source: US Mortality Data, National Center for Health Statistics, Centers for Disease Control and Prevention, 2015.
American Cancer Society, Inc., Surveillance Research, 2016
Lung and bronchus S9, page 35).19 From 2003 to 2012, incidence and death rates
Among AANHPIs, an estimated 3,460 men and 3,030 women decreased in men by about 2% annually among AANHPIs and by
will be diagnosed with lung cancer in 2016 (Figure S2). Lung about 2.5% annually among NHWs.9, 10 Among AANHPI women,
cancer is the leading cause of cancer death among both men and incidence rates were stable while death rates declined by 0.5%
women. Although incidence and mortality are roughly half that per year; in contrast, among NHW women, incidence and death
among NHWs, risk varies substantially by subgroup (Figure S3, rates decreased by about 1% annually.9, 10
page 30). The highest lung cancer incidence rate in men is in AANHPIs are more likely than NHWs to be diagnosed with lung
Samoans (98.9 per 100,000), followed by Native Hawaiians (72.1) cancer at a distant stage of disease (58% versus 52%; Figure S8,
and Vietnamese (62.7), while Asians Indians/Pakistanis have page 34); however, five-year cause-specific survival is similar
the lowest rate (21.1) (Figure S4, page 31). The highest rate in (Figure S6, page 33). AANHPIs and NHWs are equally likely to
AANHPI women is in Native Hawaiians (44.0), followed closely receive appropriate treatment for lung cancer.32 The reasons for
by Samoans (41.8), with the lowest rate also in Asian Indians/ the roughly equivalent survival in AANHPIs given later stage at
Pakistanis (10.2). diagnosis are unknown, but may include genetic and/or cultural
In the US, smoking causes 83% and 76% of all lung cancer deaths factors32 or loss of patient contact.
among men and women, respectively.26 Data on historical trends
Colon and rectum
in smoking prevalence for AANHPIs are scarce. A survey of
smoking status in 20022005 found that 42% and 27% of NHPI Among AANHPIs, an estimated 2,990 men and 2,720 women
men and women, respectively, were current smokers compared will be diagnosed with colorectal cancer in 2016 (Figure S2). It is
to 21% and 4% of Indian/Pakistani men women.27 Notably, lung the third leading cause of cancer death among both AANHPI
cancer rates among Chinese women in both Asia and the US are men and women. Incidence and death rates are 20% lower and
relatively high given the low prevalence of smoking in this group. 30% lower, respectively, compared to NHWs (Figure S3, page 30).
This may be attributable to exposure to cooking oils at high However, within AANHPI subgroups, colorectal cancer incidence
heat, secondhand smoke, genetic susceptibility, or other rates are about three times higher in Japanese than in Asian
unknown risk factors.28-31 Indians/Pakistanis (Figure S4, page 31). Higher incidence rates
among US-born compared to foreign-born Chinese and Filipi-
Since the early 1990s, when data became available, lung cancer nos in a California study are likely due to a higher prevalence of
occurrence has been decreasing among AANHPI men and behaviors associated with colorectal cancer risk, such as
relatively stable among women (Figure S7, page 33, and Figure unhealthy diet, physical inactivity, and smoking.33
AANHPI = Asian American, Native Hawaiian, and Pacific Islander. Estimates are rounded to the nearest 10, and cases exclude basal cell and squamous cell skin cancers and
in situ carcinoma except urinary bladder.
2016, American Cancer Society, Inc., Surveillance Research
Table S3. Probability (%) of Developing Invasive Cancer among AANHPIs during Selected Age Intervals by Sex,
US, 2010-2012*
Birth to 49 50 to 59 60 to 69 70 and older Birth to death
All sites Male 2.2 (1 in 46) 3.8 (1 in 26) 9.0 (1 in 11) 29.2 (1 in 3) 36.2 (1 in 3)
Female 4.5 (1 in 22) 4.7 (1 in 21) 7.1 (1 in 14) 22.6 (1 in 4) 33.3 (1 in 3)
Breast Female 1.8 (1 in 56) 2.0 (1 in 50) 2.7 (1 in 37) 4.7 (1 in 21) 10.3 (1 in 10)
Colon & rectum Male 0.3 (1 in 347) 0.6 (1 in 159) 1.2 (1 in 86) 3.9 (1 in 25) 5.3 (1 in 19)
Female 0.3 (1 in 377) 0.5 (1 in 214) 0.8 (1 in 130) 3.5 (1 in 29) 4.6 (1 in 22)
Liver & intrahepatic bile duct Male 0.2 (1 in 644) 0.4 (1 in 249) 0.6 (1 in 157) 1.7 (1 in 59) 2.6 (1 in 39)
Female <0.1 (1 in 2,828) 0.1 (1 in 1,152) 0.2 (1 in 431) 1.0 (1 in 96) 1.3 (1 in 78)
Lung & bronchus Male 0.1 (1 in 789) 0.4 (1 in 229) 1.3 (1 in 78) 6.0 (1 in 17) 6.8 (1 in 15)
Female 0.1 (1 in 823) 0.3 (1 in 318) 0.8 (1 in 128) 3.6 (1 in 28) 4.4 (1 in 23)
Prostate Male 0.1 (1 in 1,086) 0.8 (1 in 122) 3.0 (1 in 33) 7.0 (1 in 14) 9.4 (1 in 11)
Stomach Male 0.1 (1 in 1,411) 0.2 (1 in 640) 0.4 (1 in 273) 1.8 (1 in 57) 2.1 (1 in 49)
Female 0.1 (1 in 1,500) 0.1 (1 in 1,155) 0.2 (1 in 491) 1.2 (1 in 84) 1.4 (1 in 70)
Thyroid Male 0.2 (1 in 605) 0.1 (1 in 878) 0.2 (1 in 683) 0.2 (1 in 420) 0.6 (1 in 163)
Female 0.7 (1 in 136) 0.3 (1 in 291) 0.3 (1 in 302) 0.5 (1 in 209) 1.8 (1 in 55)
Uterine cervix Female 0.2 (1 in 537) 0.1 (1 in 917) 0.1 (1 in 901) 0.3 (1 in 372) 0.6 (1 in 156)
AANHPI = Asian American, Native Hawaiian, and Pacific Islander. *For those free of cancer at beginning of each age interval. All sites excludes basal and squamous cell
skin cancers and in situ cancers except urinary bladder.
Source: DevCan: Probability of Developing or Dying of Cancer Software, Version 6.7.3. Statistical Research and Applications Branch, National Cancer Institute, 2015.
http://surveillance.cancer.gov/devcan.
American Cancer Society, Inc., Surveillance Research, 2016
2 2.0 NHW men are more likely to be diagnosed with prostate cancer
1.7
at the localized stage than AANHPI men (79% versus 74%; Fig-
1 0.9 0.9 0.9 0.8 0.7 0.7 ure S8, page 34), but 5-year cause-specific survival is roughly
0.5 0.5 0.4
0
the same in both groups (Figure S6 page 33).
Naso- Stomach Liver* Thyroid Uterine Colon & Breast Lung &
pharynx cervix rectum bronchus
0
5
10
15
20
25
30
0
100
200
300
400
500
0
10
20
30
40
50
60
70
80
0
100
200
300
400
500
600
ia in ia in ia in ia in
n es n es n es n es
In e In e In e In e
di di di di
a n F ili p 7.8 a n F ili p 247.7 a n F ili p 21.7 a n F ili p 291.3 Males
, P in , P in , P in , P in
ak o ak o ak o ak o
298.9 16.7 352.2
Females
V i is t a 5.4 V i is t a V i is t a V i is t a
et et et et
na ni na ni na ni na ni
m 3.4 m 212.0 m 6.5 m 216.8
es es es es
Ko e 17.0 Ko e 257.3 Ko e 51.9 Ko e 318.6
r r r r
Ja ean Ja ean Ja ean Ja ean
pa 11.7 pa 264.1 pa 26.0 pa 313.9
Ca ne Ca ne Ca ne Ca ne
m se m se m se m se
bo 7.5 bo bo 11.7 bo 384.1
Liver
Liver
di di 303.5 di di
a a a a
All Sites
All Sites
La n La n La n La n
o 20.8 o 223.3 o 39.9 o 276.8
H a t ia n H a t ia n H a t ia n H a t ia n
wa
ii
27.6 wa
ii
238.2 wa
ii
66.1 wa
ii
377.8
S a an S a an S a an S a an
m 4.2 m 386.5 m 18.4 m 423.8
oa oa oa oa
n n n n
NH NH 442.8 NH 33.6 NH 526.5
W W W W
3.0 444.6 9.1 554.1
As Ch As Ch As Ch As Ch
0
5
10
15
20
25
0
30
60
90
120
150
0
10
20
30
40
50
0
50
100
150
200
ia in ia in ia in ia in
n es n es n es n es
In e In e In e In e
di di di 13.8 di 66.4
a n F ili p 8.4 a n F ili p 74.4 a n F ili p a n F ili p
, P in , P in , P in , P in
ak o ak o ak o ak o
V i st a i 4.9 V i st a i 100.2 V i st a i 7.4 V i st a i 101.8
et et et et
na ni na ni na ni na ni
m 4.5 m 75.6 m 5.3 m 61.2
es es es es
Ko e 11.4 Ko e 61.4 Ko e 16.0 Ko e 45.3
r r r r
Ja ean Ja ean Ja ean Ja ean
p 22.3 p 68.0 p 38.5 p 48.3
Ca ane Ca ane Ca ane C a ane
m se m se m se m se
bo 10.7 bo 105.4 bo 21.3 bo 99.9
di di di di
a a a a
Breast
La n La n La n La n
Prostate
29.1
Stomach
Stomach
o o 35.0 o o
H a t ia n H a t ia n H a t ia n H a t ia n
wa
ii
wa
ii
41.7 wa
ii
wa
ii
32.3
S a an S a an S a an S a an
m 6.1 m 135.9 m 14.0 m 101.8
oa oa oa oa
n n n n
NH NH 116.6 NH NH 169.1
W W W W
3.7 136.9 8.5 150.9
As Ch As Ch As Ch As Ch
0
5
10
15
20
25
30
0
10
20
30
40
50
60
0
1
2
3
4
5
6
7
8
0
20
40
60
80
100
ia in ia in ia in ia in
n es n es n es n es
In e In e In e In e
di di di di
a n F ili p 13.1 a n F ili p 27.6 a n F ili p 4.4 a n F ili p 46.8
, P in , P in , P in , P in
ak o ak o ak o ak o
V i is t a 23.7 V i is t a 28.6 V i is t a 7.3 V i is t a 60.2
et et et et
na ni na ni na ni na ni
m 12.6 m 10.2 m 3.2 m 21.1
es es es es
Ko e 16.3 Ko e 28.2 Ko e 3.9 Ko e 62.7
r r r r
Ja ean Ja ean Ja ean Ja ean
pa 16.9 pa 25.2 pa 4.9 pa 41.9
Ca ne Ca ne Ca ne Ca ne
m se m se m se m se
bo 10.2 bo 28.5 bo 3.6 bo 50.9
di di di di
a a a a
Thyroid
Thyroid
La n La n La n La n 46.2
o 9.8 o 26.1 o o
H a t ia n H a t ia n H a t ia n H a t ia n
Figure S4. Cancer Incidence Rates* by Sex and AANHPI Subgroup, 2006-2010
wa
ii
wa
ii
18.4 wa
ii
wa
ii
65.2
Lung & bronchus
Lung & bronchus
S a an S a an S a an S a an
m 19.8 m 44.0 m 6.9 m 72.1
oa oa oa oa
n n n n
41.8 98.9
on <25 cases are omitted. Includes intrahepatic bile duct. Please note that cancer sites are presented on different scales.
NH NH NH NH
W W W W
21.0 55.8 7.4 71.2
As Ch As Ch As Ch
0
3
6
9
12
15
0
10
20
30
40
50
0
10
20
30
40
50
60
70
80
ia in ia in ia in
n es n es n es
In e In e In e
di di di 39.1
a n F ili p 4.5 a n F ili p 31.8 a n F ili p
, P in , P in , P in
ak o ak o ak o
V i is t a 7.0 V i is t a 29.2 V i is t a 44.6
et et et
na ni na ni na ni
m 4.2 m 15.1 m 19.3
es es es
Ko e 9.5 Ko e 30.7 Ko e 39.3
r r r
Ja ean Ja ean Ja ean
pa 7.5 pa 35.9 pa 47.8
Ca ne Ca ne Ca ne
m se m se m se
bo 5.8 bo 39.4 bo 62.2
di di di
a a a
La n La n La n 46.4
o 12.7 o 34.5 o
H a t ia n H a t ia n H a t ia n
Uterine cervix
wa wa 31.3 35.4
Colon & rectum
wa
Colon & rectum
Source: Surveillance, Epidemiology, and End Results (SEER) Program, SEER 11 registries plus Greater California and New Jersey, National Cancer Institute, 2013.
ii ii ii
S a an S a an S a an
m 6.7 m 31.6 m 52.5
oa oa oa
n n n
NH NH 27.3 NH 34.4
W W W
6.8 38.8 50.5
AANHPI = Asian American, Native Hawaiian, and Pacific Islander. NHW = Non-Hispanic white. Rates are age adjusted to the 2000 US standard population. *Rates based
Male incidence
600 600
500 500
Rate per 100,000
300 300
Female incidence Male mortality
200 200
Male mortality
Female mortality
100 100
Female mortality
0 0
1990 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012 1990 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012
Year Year
AANHPI = Asian American, Native Hawaiian, and Pacific Islander. NHW = Non-Hispanic white. Rates are age adjusted to the 2000 US standard population.
Sources: Incidence- Surveillance, Epidemiology, and End Results (SEER) Program, SEER 13 registries, National Cancer Institute, 2015. Mortality- US Mortality Data, National
Center for Health Statistics, Centers for Disease Control and Prevention, 2015.
American Cancer Society, Inc., Surveillance Research, 2016
The bacterium Helicobacter pylori (H. pylori) is the strongest risk Liver
factor for stomach cancer, accounting for the majority of cases Liver cancer is one of the most fatal cancers, and incidence and
worldwide.43, 44 Other risk factors are thought to include dietary death rates among AANHPIs are about twice as high as those in
patterns, food storage and preservation practices, and low con- NHWs (Figure S3, page 30). Among AANHPIs, an estimated
sumption of fresh produce.45 Stomach cancer rates have been 1,760 men and 830 women will be diagnosed with liver cancer in
declining in the US since the early 20th century, and have also 2016 (Figure S2, page 29). It is the second-leading cause of can-
been declining more recently in Asian countries with histori- cer death among AANHPI men and the fifth-leading cause of
cally high rates, such as Japan, Korea, and China.46 These cancer death among AANHPI women. Liver cancer rates are
declines are thought to be due to improved availability of fresh particularly elevated in Laotians, Vietnamese, and Cambodians,
fruits and vegetables, lower consumption of salt-preserved likely due to a high prevalence of hepatitis B virus (HBV) infec-
foods, and reduced prevalence of H. pylori infection through tion in their country of origin and more recent immigration
improved sanitation and antibiotic treatment.47 Decreases in (Figure S4, page 31).28, 50
smoking may have also contributed to the declines.48 Stomach
cancer rates have been steadily declining among AANHPIs Chronic infection with HBV or hepatitis C virus (HCV) is the
(Figure S7, and Figure S9, page 35), with annual decreases strongest risk factor for hepatocellular carcinoma, the most
during 2003 to 2012 of about 3% to 4% for both incidence and common type of liver cancer.51 Other risk factors in Asian and
mortality.9, 10 Pacific Island nations include certain toxins and parasitic infec-
tions.52 Risk factors more common in developed countries
AANHPIs are more likely than NHWs to be diagnosed with include obesity, diabetes, alcoholic liver disease, and tobacco
stomach cancer at a localized or regional stage (Figure S8, page smoking. Risk factor prevalence varies both between and within
34), possibly because of awareness of the higher risk among AANHPI subgroups. For example, a study of Asian immigrants
Asian Americans and/or recommendations by some medical in New York City found that those born in Fujian Province,
societies for screening among Asian immigrants.49 Likely due to China, were more likely to have HBV infection than those born
earlier diagnosis, AANHPIs have higher 5-year survival than in other Chinese provinces.53
NHWs, 40% versus 28% in males and 38% versus 34% in females
(Figure S6).
38
Filipinos are not well understood, but are thought to include
40 34
26 25
dietary or environmental factors.57
23
20
20
0
All sites Thyroid Breast Uterine
cervix
Colon &
rectum
Naso-
pharynx
Stomach Liver* Lung &
bronchus
Figure S7. Trends in Cancer Incidence Rates among
AANHPIs by Site and Sex, 1992-2012
AANHPI = Asian American, Native Hawaiian, and Pacific Islander. Males
NHW = Non-Hispanic white. *Includes intrahepatic bile duct. 140
Source: Surveillance, Epidemiology, and End Results (SEER) Program, Prostate
SEER 18 registries, National Cancer Institute, 2015. 120
American Cancer Society, Inc., Surveillance Research, 2016
100
Rate per 100,000
80
Liver cancer is one of the few cancers for which incidence and 60
Lung & bronchus
medical equipment and injection drug use during the 1960s and 80
1970s, and possibly increases in obesity and type 2 diabetes
60
more recently.54 Cultural awareness of HBV screening and treat- Lung & bronchus
Colon & rectum
ment among AANHPIs, who have historically had the highest 40
liver cancer rates in the US, may be driving the declining mortal- Thyroid
20 Stomach Liver*
ity rates.54
0
AANHPIs are more likely than NHWs to be diagnosed with liver 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012
Year
cancer at a localized stage (46% versus 42%; Figure S8, page
Rates are age adjusted to the 2000 US standard population. *Includes
34) and also have higher five-year survival rates (Figure S6). intrahepatic bile duct.
Better survival among AANHPIs may be due to earlier stage at Source: Surveillance, Epidemiology, and End Results (SEER) Program, SEER 13
diagnosis, differences in receipt of treatment, and/or other registries, National Cancer Institute, 2015.
American Cancer Society, Inc., Surveillance Research, 2016
underlying risk factors, such as cirrhosis.55, 56
100 2% 2% 2% 2%
4% 3% 5% 5% 5% 6% 6% 7%
7% 6% 5% 5%
5% 14% 13% 12% 11%
6% 13% 13%
12% 19% 19%
26%
80 12% 29% 29% 16%
33% 18% 28%
34%
32% 52%
58%
39%
60 26% 35% 36%
26%
Percent
31%
40 79% 26%
74%
69% 65%
64% 22%
60%
51% 19%
43% 42% 46%
20 40% 40%
29% 30%
19%
16%
0
NHW AANHPI NHW AANHPI NHW AANHPI NHW AANHPI NHW AANHPI NHW AANHPI NHW AANHPI NHW AANHPI
Prostate Thyroid Female Uterine Liver* Colon & Stomach Lung &
breast cervix rectum bronchus
AANHPI = Asian Americans, Native Hawaiians, and Pacific Islanders. NHW = Non-Hispanic whites. Based on rates age adjusted to the 2000 US standard population.
*Includes intrahepatic bile duct.
Source: Surveillance, Epidemiology, and End Results (SEER) Program, SEER 18 registries, National Cancer Institute, 2015.
American Cancer Society, Inc., Surveillance Research, 2016
Thyroid cancer incidence rates have been increasing by more second half of the 20th century, including those since 1990
than 5% annually over the past 10 years of data among both among Vietnamese, Cambodian, and Laotian women, are attrib-
AANHPIs and NHWs (Figure S7, page 33).9 The increasing uted primarily to increased screening.65
incidence is thought to be partially due to increased detection
Incidence and death rates among AANHPIs decreased by about
because of more sensitive diagnostic procedures and increased
3% annually during the past 10 years of data, while incidence
use of imaging, although incidental detection of thyroid tumors
rates decreased slightly and mortality rates remained stable in
is unlikely to completely account for these trends.58, 59 Increases
NHW women.9, 10 AANHPI women are less likely than NHW
across demographic and socioeconomic groups, as well as for
women to be diagnosed with cervical cancer at a localized stage
larger and later-stage tumors, also implicate environmental fac-
(43% versus 51%), although five-year survival is about 70% for
tors.60 Further research is needed to identify risk factors that
both groups (Figures S6, page 33, and S8).
may be causing these trends.
Nasopharynx
Uterine cervix
Nasopharyngeal carcinoma, which is the dominant form of
Cervical cancer incidence rates are higher in several AANHPI
nasopharyngeal cancer, is rare worldwide, although it has ele-
subgroups than in NHWs (Figure S4, page 31), despite being
vated incidence in certain regions and populations, including
lower overall (Figure S3, page 30). Incidence rates (per 100,000)
southern China and southeastern Asia.47 (The nasopharynx is
are twice as high in Cambodians (12.7) as in NHWs (6.8), and
the upper part of the throat, behind the nose.) Incidence rates
40% higher among Vietnamese women (9.5). In contrast, rates
among AANHPIs overall are about 5 to 6 times higher than
among Chinese (4.5) and Asian Indian/Pakistani (4.2) women
among NHWs (Figure S3, page 30), and are particularly ele-
are lower than those in NHWs.
vated for men in certain subpopulations, including Chinese,
Contemporary disparities in cervical cancer incidence world- Samoans, Guamanians/Chamorros, and Hmong.66-69 Nasopha-
wide are attributable to differences in the prevalence of both ryngeal carcinoma is thought to be caused by a combination of
human papillomavirus (HPV) infection, the cause of cervical viral, environmental, and genetic factors.70 It has been estimated
cancer, and screening.61-64 The Pap test has historically been the that about 98% of nasopharyngeal carcinoma cases worldwide
mainstay for screening in the US and can detect precancerous are related to infection with Epstein-Barr virus (EBV),47 although
lesions of the cervix that can be treated to prevent cancer. The only a small fraction of people who are infected with EBV
rapid declines in cervical cancer occurrence in the US over the develop the disease. Other environmental risk factors include
30 Tobacco
Smoking among AANHPIs varies by sex, nativity, acculturation,
20 and ethnicity. Overall, 10% of Asian Americans smoked in 2014,
Liver* Colon & rectum
15
ences reflect smoking norms in home countries, where smoking
Breast
is more accepted among men than women, and acculturation in
10
Colon & rectum
the US.5 Among the three largest Asian American ethnic groups,
current smoking is more common among Filipinos (12%) than
5 Liver*
Chinese (7%) or Asian Indians (6%) (Table S4, page 36). A study
Stomach
of Asians in New York found smoking rates as high as 36% in
0 Korean men.80 Notably, while current smoking among NHWs is
1990 1992 1994 1996 1998 2000 2002 2004 2006 2008 2010 2012
most common among those with lower income and/or less edu-
Year
Rates are age adjusted to the 2000 US standard population. *Includes
cation and the same is true for Asian American men, the reverse
intrahepatic bile duct. is true for Asian American women.81
Source: US Mortality Data, National Center for Health Statistics, Centers for
Disease Control and Prevention, 2015. Smoking prevalence in Asian American men decreased from
American Cancer Society, Inc., Surveillance Research, 2016
25% in 1990-1992 to 14% in 2014, while in women, it has remained
stable at 6% (Figure S10, page 37). However, national trends do
not necessarily reflect those among specific groups or localities.
smoking, alcohol consumption, occupational exposures, and For instance, there was no decline in smoking among Asian
certain preserved foods.71 Cantonese salted fish, which is high in males in New York City from 2002 to 2010.82
nitrosamines, was identified as a risk factor for nasopharyngeal
carcinoma among southern Chinese in the 1970s,72 leading to its Overweight/obesity
designation by the International Agency for Research on Cancer Excess body weight increases the risk of several cancers, and
as a carcinogen.73 also contributes to the development of other cancer risk factors,
such as nonalcoholic fatty liver disease and type 2 diabetes.
Incidence and mortality rates for nasopharyngeal carcinoma in
Worldwide, normal weight is defined as a body mass index (BMI,
AANHPIs declined by about 2% to 3% annually from 2003 to
kg/m2) of 18.5-24.9, while overweight is 25-29.9 and obese is 30.
2012.9, 10 Rates have also been declining among some high-risk
However, it has been shown that Asians have a higher percent-
populations in Asia, possibly due to decreased smoking or con-
age of body fat than whites at the same BMI, as well as a higher
sumption of salted fish.74, 75 The recent declines among AANHPIs
risk for type 2 diabetes at a lower BMI.83 As a result, lower BMI
are not well understood, but may be attributable to dietary fac-
cutpoints established by the American Diabetes Association are
tors and decreased smoking.74 Five-year cause-specific survival
used for assessing diabetes risk in Asian Americans.84, 85 Diabe-
is higher for AANHPIs than NHWs (males 66% versus 59%;
tes is a risk factor for several cancers, including breast, liver,
females 74% versus 58%; Figure S6, page 33) for reasons that
pancreatic, and colorectal.86 While some studies report elevated
are unknown, but may include lower prevalence of other health
cancer risk at a lower BMI among Asians compared with other
conditions and/or less complete follow-up of AANHPI patients
populations, especially for colon cancer,87, 88 others do not.89, 90
after diagnosis.11, 76
BMI = Body mass index. *Estimates from 2013-2014 data combined. Moderate: 12+ drinks in lifetime and (male) 3-14 drinks/week in past year or (female) 3-7 drinks/
week in past year. Heavy: 12+ drinks in lifetime and (male) >14 drinks/week in past year or (female) >7 drinks/week in past year. Aerobic activity recommendations:
includes 150 minutes of moderate intensity activity or 75 minutes of vigorous intensity activity each week. Estimate not provided due to instability. Note: Percentages
are age adjusted to the 2000 U.S. standard population.
Sources: All risk factors except BMI National Center for Health Statistics. National Health Interview Survey, 2013 and 2014. Public-use data file. BMI National Center
for Health Statistics. National Health and Nutrition Examination Survey Data, 2013-14.
American Cancer Society, Inc., Surveillance Research, 2016
Three large pooled studies did not find Asians to be at higher Alcohol
risk for cancer death at a lower BMI.91-93 Thus, evidence to date is Alcohol consumption is associated with increased risk of several
inconclusive about whether cancer risk is increased in Asians at cancers, and it also may interact with HBV and HCV to further
a lower BMI. promote the development of liver cancer.97 This is of special con-
Asian Americans are much more likely to be a healthy weight cern among Asian Americans, who bear a disproportionate
than NHWs.94 About 42% of Asian Americans are overweight or burden of HBV infection. Asian Americans are half as likely as
obese compared to 69% of NHWs (Table S4). In contrast, three- NHWs to be moderate drinkers; however, prevalence among US-
quarters of Native Hawaiians in Hawaii are overweight or born Asian Americans (16%) approaches that of NHWs (18%)
obese.79 Asian American men (50%) are more likely to be over- (Table S4).
weight or obese than Asian American women (35%). Excess body
weight has increased among US-born Asian Americans, as well
Infectious agents
as recent and long-term immigrants. For instance, the preva- H. pylori
lence of overweight among US-born Filipinos increased from Chronic infection with H. pylori is highly endemic in Asia and
36% in 1992-1995 to 55% in 2003-2008.95 Prevalence of over- prevalence patterns mirror gastric cancer risk.98 H. pylori sero
weight and obesity varies by Asian American subgroup; a study prevalence is close to 60% in China and Korea,98 whereas it is
in California found that only 8% of South Asian and 9% of Chi- about 30% in the United States, where H. pylori infection has been
nese children were overweight, compared to 16% of Japanese declining since the late 19th century.99, 100 Although the spread of
and Korean children and 18% of Filipino children.96 H. pylori is not well understood, infection occurs primarily dur-
ing childhood and risk is higher in lower socioeconomic groups.100
Among Japanese immigrants to the US in the 1970s and 1980s,
Percent
were born or have parents who were born in a country where 15
Asian men
HBV is highly prevalent.104 AANHPIs account for more than 50%
10
of those infected with HBV in the United States, although most
who harbor the virus are unaware.104 The HBV vaccine was Asian women
5
introduced in the early 1980s and has resulted in dramatic
declines in liver cancer incidence among vaccinated cohorts in
0
Taiwan.105 HBV vaccination in the US among AANHPI teens 1990-1992 1993-1995 1999-2001 2006-2008 2009-2011 2011-2013 2014
(86%) is slightly lower than other racial/ethnic groups, which all Year
have HBV vaccination coverage above 90%.106 The United States
Preventive Services Task Force (USPSTF) recommends screen- *Estimates are age adjusted to the 2000 US standard population.
Source: 1990-2013: Health, United States, 2014: With Special Feature on
ing all those born in regions with a prevalence of HBV infection Adults Aged 55-64.6 2014: Centers for Disease Control and Prevention.
2%, which includes all countries of Asia and the Pacific Islands National Health Interview Survey, 2014. Public-use data file.
except Australia and New Zealand.107 Among adults 18 years of American Cancer Society, Inc., Surveillance Research, 2016
age and older, about 28% of both Asian Americans and NHWs
had received a hepatitis B test (Table S5, page 38).
girls 13-17 years of age, 36% received the three recommended
While HBV is the leading liver cancer risk factor among Asian doses and 72% of those who received the first dose completed all
Americans in the US, HCV is also an important risk factor, espe- three doses, similar to uptake among NHWs (Table S5, page
cially in some groups.108-110 For example, HCV is more common 38). HPV vaccination uptake in Asian American boys is higher
than HBV in Japan, where about 65% of liver cancers are esti- than in NHWs, with 27% receiving the three recommended
mated to be attributable to HCV;111 however, HCV prevalence doses (compared with 19% in NHW boys) and 63% completion
there has been decreasing due to public health programs.112 HCV (compared with 58% in NHW boys) (Table S5, page 38). HPV
is also more prevalent in Pakistan and among older adults in vaccine uptake is influenced by caregiver awareness and varies
Taiwan.108 The USPSTF also recommends HCV screening for all by local context; in a study in Los Angeles, California, only 64%
adults born between 1945 and 1965, who account for three- and 44% of Chinese and Korean mothers, respectively, with age-
quarters of HCV-infected individuals and HCV-related deaths in eligible daughters were aware of the vaccine.117
the United States.113 HCV testing coverage in this cohort is 13%
among NHWs and 10% among Asian Americans (Table S5, page
38). Through testing, HBV and HCV can be detected and Prevalence of cancer screening
treated, reducing the risk of liver cancer.114 Cervical and colorectal screening can detect and remove pre-
cancerous lesions, thus preventing the development of cancer. In
HPV addition, screening for colorectal, cervical, and breast cancer
HPV causes nearly all cervical cancers in the US, as well as many can detect cancers at an earlier stage when more treatment
oropharyngeal and anogenital cancers.115 A clinic-based study options are available. Please see page 66 for screening recom-
in 2003-2005 found that 17% of AANHPI women had a high-risk mendations for people at average cancer risk.
HPV infection (the type most likely to cause cancer), compared
with 23% of white women.116 More recent HPV prevalence data Asian Americans are less likely than NHWs to be current for cer-
are not available for AANHPI in the US. Worldwide, it is esti- vical and colorectal cancer screening, but have similar rates of
mated that 5% of women in North America are infected with any breast cancer screening (Table S5). Seventy-one percent of Asian
type of HPV, compared with 11% of women in Eastern Asia, 7% in American women overall (21-65 years of age) reported having a
Southern Asia, and 14% in Southeastern Asia.61 Vaccines to pre- Pap test within the past 3 years, compared with 83% of NHWs.
vent infection with the most common cancer-causing types of However, prevalence varies widely by subgroup and in Filipinas
HPV have been available since 2006 and are recommended for is equal to that in NHWs. Slightly more than two-thirds of Asian
boys and girls at 11 to 12 years of age. Among Asian American American (68%) and NHW (69%) women 45 years of age or older
report having a mammogram within the past two years. Only Asian Americans of lower socioeconomic status are less likely to
about half of Asian Americans (52%) 50 years of age and older receive recommended cancer screening, often because of less
received recommended colorectal cancer screening, compared access to health care.119 Among Asian Americans, 13% of adults
with 61% of NHWs. Notably, this disparity is almost entirely 18-64 years of age were uninsured in 2014, including 16% of those
driven by the low screening rate among Asian American women. who were foreign-born, while 21% of men and 14% of women had
While endoscopy is generally the preferred screening test among no regular source of medical care (Table S4, page 36). Among
both NHWs and Asian Americans, Asian Americans are more Native Hawaiians in Hawaii, 8% were uninsured and 16% had no
likely than NHWs to have had a fecal occult blood test (11% ver- regular source of medical care.79 Successful interventions to pro-
sus 7%) and less likely to have had endoscopy (48% versus 58%) mote cancer screening among Asian Americans utilize lay health
(Table S5). A recent study reported that Native Hawaiians were workers, one-on-one communications, translated materials, and
more than 30% less likely to get a colonoscopy or mammogram approaches that not only involve Asian community members,
compared to NHWs.118 but also health care providers.120 Patient navigators in particular
have been shown to improve the receipt of recommended screen-
ing and follow-up.121
Figure 4. Number and Percentage (%) of Cancer Deaths Attributable to Cigarette Smoking in 2011,
Adults 35 Years and Older
Attributable to cigarette smoking Other causes
Men Women
Lung, bronchus, & trachea 83% Lung, bronchus, & trachea 76%
Esophagus 52% Pancreas 14%
0 20 40 60 80 100 0 20 40 60 80 100
Number of deaths (in thousands) Number of deaths (in thousands)
Mortality
All sites
Male 210.6 267.7 128.4 186.7 148.0
Female 149.2 170.4 91.2 133.9 99.4
Breast (female) 21.9 31.0 11.4 15.0 14.5
Colon & rectum
Male 18.2 27.6 13.0 18.8 15.6
Female 12.9 18.2 9.4 15.6 9.6
Kidney & renal pelvis
Male 5.9 5.7 2.9 8.7 5.0
Female 2.6 2.6 1.2 4.7 2.4
Liver & intrahepatic bile duct
Male 7.6 12.8 14.5 13.9 12.9
Female 3.1 4.4 6.1 6.3 5.6
Lung & bronchus
Male 62.2 74.9 34.0 49.1 29.5
Female 41.4 36.7 18.2 32.1 13.7
Prostate 19.9 47.2 9.4 20.2 17.8
Stomach
Male 3.6 9.4 7.9 7.4 7.2
Female 1.8 4.5 4.7 3.6 4.2
Uterine cervix 2.0 4.1 1.8 3.5 2.7
Hispanic origin is not mutually exclusive from Asian/Pacific Islander or American Indian/Alaska Native. *Rates are per 100,000 population and age adjusted to the 2000
US standard population. Data based on Indian Health Service Contract Health Service Delivery Areas. Incidence rates exclude data from Kansas.
Source: Incidence North American Association of Central Cancer Registries, 2015. Mortality US mortality data, National Center for Health Statistics, Centers for
Disease Control and Prevention, 2015.
American Cancer Society, Inc., Surveillance Research, 2016
Males
WA
MT ND ME
OR MN VT
ID NH
SD MA
WI NY
WY
MI RI
CT
IA PA
NV NE NJ
OH
UT IL IN DE
CA CO WV MD Rate per 100,000 males
KS VA
MO DC 26.4 - 46.6
KY
NC 46.7 - 58.2
TN
AZ OK 58.3 - 68.0
NM AR SC 68.1 - 77.4
MS AL GA 77.5 - 92.2
AK
TX LA
FL
HI
Females
WA
MT ND ME
OR MN VT
ID NH
SD MA
WI NY
WY
MI RI
CT
IA PA
NV NE NJ
OH
UT IL IN DE
CO
Rate per 100,000 females
CA WV MD
KS VA
MO DC 15.6 - 27.2
KY
27.3 - 35.8
NC
TN
AZ OK 35.9 - 41.4
NM AR SC 41.5 - 45.3
MS AL GA 45.4 - 55.2
AK
TX LA
FL
HI
Sources of Statistics
Estimated new cancer cases in 2016. The number of new can- period divided by the number of people who were at risk for the
cer cases in the US in 2016 was projected using a spatiotemporal disease in the population. Incidence rates in this publication are
model based on incidence data from 49 states and the District of presented per 100,000 people and are age adjusted to the 2000
Columbia for the years 1998-2012 that met the North American US standard population to allow comparisons across popula-
Association of Central Cancer Registries (NAACCR) high-qual- tions with different age distributions. State-, race-, and
ity data standard for incidence. This method considers ethnicity-specific incidence rates were previously published in
geographic variations in sociodemographic and lifestyle factors, NAACCRs publication Cancer Incidence in North America, 2008-
medical settings, and cancer screening behaviors as predictors 2012. (See B in Additional information on page 65 for full
of incidence, and also accounts for expected delays in case reference.)
reporting. (For more information on the estimation of new inva-
Trends in cancer incidence rates provided in this publication are
sive cases, see A in Additional information on page 65.)
based on delay-adjusted incidence rates from registries in the
The number of new cases among Asian Americans, Native National Cancer Institutes Surveillance, Epidemiology, and End
Hawaiians, and Pacific Islanders (AANHPIs), as well as those for Results (SEER) program. Delay-adjustment accounts for delays
female breast carcinoma in situ and melanoma in situ, were esti- and error corrections that occur in the reporting of cancer cases,
mated by projecting the average annual percent change in the which is substantial for some sites, particularly those less often
estimated number of cases during the most recent 10 years of diagnosed in a hospital, such as leukemia. Delay-adjustment is
data (2003-2012) to 2016. Cases from 2003 through 2012 were not available for some cancer types. Trends were originally pub-
estimated by applying age-specific incidence rates from 44 lished in the SEER Cancer Statistics Review (CSR) 1975-2012. (See
states and the District of Columbia to population counts. Esti- C in Additional information on page 65 for full reference.)
mates for AANHPIs were adjusted for delays in case reporting.
Estimated cancer deaths in 2016. The estimated number of US
Delay adjustment was unavailable for in situ breast and in situ
cancer deaths was calculated by fitting the number of cancer
melanoma estimates.
deaths from 1998 to 2012 to a statistical model that forecasts the
Incidence rates. Incidence rates are defined as the number of number of deaths expected to occur in 2016. The estimated
people who are diagnosed with cancer during a given time number of cancer deaths for each state was calculated similarly
Breast Women, Mammography Women should undergo regular screening mammography starting at age 45 years.
ages 40-54 Women ages 45 to 54 should be screened annually.
Women should have the opportunity to begin annual screening between the ages of 40 and 44.
Women, Transition to biennial screening, or have the opportunity to continue annual screening.
ages 55+ Continue screening as long as overall health is good and life expectancy is 10+ years.
Cervix Women, Pap test Screening should be done every 3 years with conventional or liquid-based Pap tests.
ages 21-29
Women, Pap test & HPV DNA test Screening should be done every 5 years with both the HPV test and the Pap test (preferred),
ages 30-65 or every 3 years with the Pap test alone (acceptable).
Women, Pap test & HPV DNA test Women ages 66+ who have had 3 consecutive negative Pap tests or 2 consecutive negative
ages 66+ HPV and Pap tests within the past 10 years, with the most recent test occurring in the past 5
years should stop cervical cancer screening.
Colorectal Men and Guaiac-based fecal occult Annual testing of spontaneously passed stool specimens. Single stool testing during a clinician
women, blood test (gFOBT) with office visit is not recommended, nor are throw in the toilet bowl tests. In comparison with
ages 50+ at least 50% sensitivity guaiac-based tests for the detection of occult blood, immunochemical tests are more patient-
or fecal immunochemical friendly and are likely to be equal or better in sensitivity and specificity. There is no justification
test (FIT) with at least 50% for repeating FOBT in response to an initial positive finding.
sensitivity, OR
Flexible sigmoidoscopy Every 5 years alone, or consideration can be given to combining FSIG performed every 5
(FSIG), OR years with a highly sensitive gFOBT or FIT performed annually.
Endometrial Women at Women should be informed about risks and symptoms of endometrial cancer and encouraged
menopause to report unexpected bleeding to a physician.
Lung Current or Low-dose helical CT Clinicians with access to high-volume, high-quality lung cancer screening and treatment centers
former smokers (LDCT) should initiate a discussion about annual lung cancer screening with apparently healthy patients
ages 55-74 in ages 55-74 who have at least a 30 pack-year smoking history, and who currently smoke or have
good health quit within the past 15 years. A process of informed and shared decision making with a clinician
with 30+ pack- related to the potential benefits, limitations, and harms associated with screening for lung cancer
year history with LDCT should occur before any decision is made to initiate lung cancer screening. Smoking
cessation counseling remains a high priority for clinical attention in discussions with current
smokers, who should be informed of their continuing risk of lung cancer. Screening should not
be viewed as an alternative to smoking cessation
Prostate Men, Prostate-specific antigen Men who have at least a 10-year life expectancy should have an opportunity to make an
ages 50+ test with or without digital informed decision with their health care provider about whether to be screened for prostate
rectal examination cancer, after receiving information about the potential benefits, risks, and uncertainties
associated with prostate cancer screening. Prostate cancer screening should not occur without
an informed decision-making process.
CT-Computed tomography. *All individuals should become familiar with the potential benefits, limitations, and harms associated with cancer screening. All positive tests
(other than colonoscopy) should be followed up with colonoscopy.
Acknowledgments
The production of this report would not have been possible without the efforts of: Rick Alteri, MD; Tracie
Bertaut, APR; Durado Brooks, MD, MPH; William Chambers, PhD; Ellen Chang, ScD; Moon S. Chen, Jr., PhD,
MPH; Sally Cowal, MPA; Dennis Deapen, DrPH, MPH; Carol DeSantis, MPH; Colleen Doyle, MS, RD; Jeffrey
Drope, PhD; Stacey Fedewa, MPH; Ted Gansler, MD, MBA; Susan Gapstur, PhD; Mia Gaudet, PhD; Ann
Goding-Sauer, MSPH; Scarlett Lin Gomez, PhD, MPH; Brenda Y. Hernandez, PhD, MPH; Eric Jacobs, PhD;
Marjorie Kagawa-Singer, RN, PhD; Debbie Kirkland; Lihua Liu, PhD, MS; Joannie Lortet-Tieulent, MSc;
Melissa Maitin-Shepard, MPP; Ann McMikel, MA; Anne-Michelle Noone, MS; Meg OBrien, PhD; Anthony
Piercy; Paulo Pinheiro, MD, PhD; Ken Portier, PhD; Debbie Saslow, PhD; Scott Simpson; Robert Smith, PhD;
Kevin Stein, PhD; Lindsey Torre, MSPH; Dana Wagner; Sophia Wang, PhD; Elizabeth Ward, PhD; Martin
Weinstock, MD; and Joe Zou.
Cancer Facts & Figures is an annual publication of the American Cancer Society, Atlanta, Georgia.
For more information, contact:
Rebecca Siegel, MPH; Kimberly Miller, MPH; or Ahmedin Jemal, DVM, PhD
Surveillance and Health Services Research Program
2016, American Cancer Society, Inc.
No. 500816